Canonical Allele Identifier: PA2825861259
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2193352
ClinVar RCV Id: RCV002623939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137462.1:p.Ser125Pro
CA397859203
NM_001143990.2:c.373T>C